State

Northern Mariana Islands product recalls

73,598 recalls have nationwide distribution and so reach Northern Mariana Islands. 23 additional recalls listed Northern Mariana Islands specifically in their distribution scope.

What the numbers show

Total: 23
Critical: 0
Severe: 18
Most recent: 2026-09-23

Of the 23 recalls naming Northern Mariana Islands we have scored against our rubric, 0 (0%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 18 (78%) are Severe.

Which agencies issued them

These figures cover only the 23 recalls whose distribution notice names Northern Mariana Islands specifically. The 73,598 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

29751–29775 of 73621

HighFDA (Devices)·Z-1317-2020·2020-02-26
Nobel Biocare Implant Retrieval Instruments Recalled for Sterility Concerns
Nobel Biocare is recalling 197 implant retrieval instruments because a packaging defect may compromise sterility during shelf life.
Product
Implant Retrieval Instrument Hex & Tri-Chi NP/RP 31mm - Product Usage: They can be used to remove implants, if the implant connection has been damaged. It can be used to remove implants with internal conical connection, internal tri-channel connection or external hex connection.
Category
Medical Device
Distribution
Distributed nationwide
HighCPSC·20079·2020-02-26
Home Depot Recalls 4-Drawer Whitewash Chests Due to Tip-Over Hazards
Home Depot is recalling approximately 200 4-Drawer Whitewash Chests because they are unstable if not anchored to the wall, posing tip-over and entrapment hazards.
Product
Home Decorators Collection Print Block 4-Drawer Whitewash Chest
Category
Consumer Product
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1274-2020·2020-02-26
Recall of Polysorb Braided Absorbable Suture Due to Packaging Integrity Issues
Covidien LLC is recalling specific lots of Polysorb Braided Absorbable Suture due to potential packaging integrity issues that may impact the humidity or sterility barrier.
Product
Polysorb Braided Absorbable Suture 3/0 VIOLET 30" CV-24 (75CM), Item Code CL461 - Product Usage: Indicated for use in soft tissue approximation or ligation and ophthalmic surgery, but not in cardiovascular or neural tissue.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-0709-2020·2020-02-26
Taspen's Organics Respiratory Tea Recalled Due to Coltsfoot Ingredient
Green Water, LLC is recalling Taspen's Organics Respiratory Tea because it contains Coltsfoot, an ingredient not intended for internal use.
Product
Taspen's Organics Respiratory Tea, sold in 2 oz packages
Category
Food
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1301-2020·2020-02-26
Cardinal Health Recalls Presource Procedure Packs Due to Sterility Concerns
Cardinal Health is recalling Presource Procedure Packs containing AAMI Level 3 surgical gowns because they may not be sterile. This could increase the risk of surgical site infections.
Product
Presource Procedure Packs containing AAMI Level 3 surgical gowns, Multiple Catalog Numbers Produced Between September 1, 2018 and January 15, 2020
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1279-2020·2020-02-26
Recall of Polysorb Braided Absorbable Suture Due to Packaging Integrity Issues
Covidien LLC is recalling specific lots of Polysorb Braided Absorbable Suture 13-0 due to potential packaging integrity issues that may impact sterility.
Product
Polysorb Braided Absorbable Suture 13-0 VIOLET 30" GS-23, Item Code CL892 - Product Usage: Indicated for use in soft tissue approximation or ligation and ophthalmic surgery, but not in cardiovascular or neural tissue.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1338-2020·2020-02-26
Siemens Luminos Agile Max Recalled for Software Bug Affecting Patient Images
Siemens is recalling 475 Luminos Agile Max devices due to a software bug that may assign one image to two patients, potentially affecting diagnosis.
Product
Luminos Agile Max, model no. 10762471 - Product Usage: Luminos Agile Max is a device intended to visualize anatomical structures by converting an X-ray pattern into a visible image. The system has medical applications ranging from gastrointestinal examinations to cranial…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1303-2020·2020-02-26
Nobel Biocare Recalls Tapered Dental Drills Due to Sterility Concerns
Nobel Biocare is recalling 8 units of tapered dental drills because a packaging sealing issue may compromise sterility during shelf life.
Product
Drill Tapered NP 3.5x8 mm Single-Pat - Product Usage: The Guided Drills (Twist (Step) Drills, Guided Tapered Drills) are used for preparing osteotomies for the specific related implants.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1260-2020·2020-02-26
Siemens Recalls ADVIA Chemistry CardioPhase hsCRP Calibrator Due to Accuracy Drift
Siemens Healthcare Diagnostics is recalling 844 units of ADVIA Chemistry CardioPhase hsCRP Calibrator because accuracy has drifted from reference materials, causing high bias in quality control and patient sample recovery.
Product
ADVIA Chemistry CardioPhase High Sensitivity C-Reactive Protein (hsCRP) Calibrator - product Usage: For in vitro diagnostic use in the calibration of ADVIA¿ Chemistry systems for the CardioPhase¿ hsCRP assay.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1232-2020·2020-02-26
Siemens Dimension Enzymatic Creatinine Reagent Recalled for Interference
Siemens Healthcare Diagnostics is recalling Dimension Enzymatic Creatinine reagent because it may produce falsely low results for patients taking phenindione.
Product
Dimension Enzymatic Creatinine (EZCR) reagent, SMN 10471520
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-0730-2020·2020-02-26
Safeway Cream Cheese Icing Recalled for Plastic Polymer Contamination
CSM Bakery Products is recalling 32 lb. pails of Safeway Cream Cheese Icing because pieces of plastic polymer were introduced into the sugar system.
Product
32 lb. pail SAFEWAY CREAM CHEESE ICING, MDM # 10203458, Distributed by Safeway Inc. PO Box 99 Pleasanton, CA 94566-0009
Category
Food
Distribution
Distributed nationwide
HighFDA (Food)·F-0720-2020·2020-02-26
CSM Bakery Products Recalls Frozen Chocolate Chip Cookie Dough Due to Plastic
CSM Bakery Products is recalling specific lots of frozen chocolate chip cookie dough because pieces of plastic polymer were introduced into the sugar system.
Product
30 lb. cases of 480 1.0 oz frozen chocolate chip cookie dough, MDM # 10194622, Manufactured by Brill Inc. Tucker, GA 30084 1 866 982 7455 OR BRILLINC.COM
Category
Food
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1328-2020·2020-02-26
Philips CombiDiagnost GCF X-ray System Software Recall
Philips is recalling 116 CombiDiagnost GCF X-ray systems due to a software error that locks the table and an incorrectly installed thermos switch.
Product
CombiDiagnost GCF, Software v. 1.0.5, Product Code 709030 - Product Usage: Xray system, diagnostic, fluoroscopic, general purpose.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1231-2020·2020-02-26
Siemens Atellica CH Enzymatic Creatinine Reagent Recalled for Interference
Siemens Healthcare Diagnostics is recalling Atellica CH Enzymatic Creatinine reagent due to potential falsely depressed results for patients on phenindione therapy.
Product
Atellica CH Enzymatic Creatinine (ECRE_2) reagent, SMN 11097533
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1339-2020·2020-02-26
Siemens Ysio Max Radiographic System Recalled for Software Bug
Siemens Medical Solutions is recalling 507 Ysio Max radiographic systems because a software bug may assign one image to two different patients, potentially affecting medical diagnosis.
Product
Ysio Max, model no. 10762470 - Product Usage: The Ysio Max is a radiographic system used in hospitals, clinics, and medical practices. Ysio Max enables radiographic and tomographic exposures f the whole body including: skull, chest, abdomen, and extremities and may be used on…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1275-2020·2020-02-26
Polysorb Suture Recall Due to Packaging Integrity Issues
Covidien LLC is recalling specific lots of Polysorb Braided Absorbable Suture due to potential packaging integrity issues that may impact sterility.
Product
Polysorb Braided Absorbable Suture 0 30" UNDYED HOS-11, Item Code CL537 - Product Usage: Indicated for use in soft tissue approximation or ligation and ophthalmic surgery, but not in cardiovascular or neural tissue.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1280-2020·2020-02-26
Recall of Polysorb Braided Absorbable Suture Due to Packaging Integrity Issues
Covidien LLC is recalling specific lots of Polysorb Braided Absorbable Suture due to potential packaging integrity issues that may impact the humidity or sterility barrier.
Product
Polysorb Braided Absorbable Suture 2 36" VIOLET GS-24, Item Code CL911 - Product Usage: Indicated for use in soft tissue approximation or ligation and ophthalmic surgery, but not in cardiovascular or neural tissue.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1307-2020·2020-02-26
Nobel Biocare Recalls Tapered Drills Due to Sterility Concerns
Nobel Biocare is recalling 473 tapered dental drills because a packaging defect may compromise sterility during shelf life.
Product
Drill Tapered NP 3.5x11.5 mm Single-Pat - Product Usage: The Guided Drills (Twist (Step) Drills, Guided Tapered Drills) are used for preparing osteotomies for the specific related implants.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1293-2020·2020-02-26
FDA Recalls Polysorb Suture Due to Packaging Integrity Concerns
The FDA is recalling specific lots of Polysorb Braided Absorbable Suture due to potential packaging integrity issues that could impact sterility.
Product
Polysorb Braided Absorbable Suture 6/0 18" UNDYED P-10, Item Code SL1625G - Product Usage: Indicated for use in soft tissue approximation or ligation and ophthalmic surgery, but not in cardiovascular or neural tissue.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1308-2020·2020-02-26
Nobel Biocare Guided Tapered Drills Recalled for Sterility Concerns
Nobel Biocare is recalling 346 Guided Tapered Drills because a packaging sealing issue may compromise sterility during shelf life.
Product
Drill Tapered RP 4.3x10 mm Single-Pat - Product Usage: The Guided Drills (Twist (Step) Drills, Guided Tapered Drills) are used for preparing osteotomies for the specific related implants.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1276-2020·2020-02-26
FDA Recalls Polysorb Sutures Due to Packaging Integrity Concerns
The FDA is recalling specific lots of Polysorb Braided Absorbable Sutures due to potential packaging integrity issues that could compromise sterility.
Product
Polysorb Braided Absorbable Suture 2/0 30 VIOLET GS-21, Item Code CL811 - Product Usage: Indicated for use in soft tissue approximation or ligation and ophthalmic surgery, but not in cardiovascular or neural tissue.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1305-2020·2020-02-26
Nobel Biocare Recalls Screw Taps Due to Packaging Seal Defects
Nobel Biocare is recalling Screw Tap Tapered WP Single-Pat devices because a packaging sealing defect may compromise sterility during shelf life.
Product
Screw Tap Tapered WP Single-Pat - Product Usage: The Guided Drills (Twist (Step) Drills, Guided Tapered Drills) are used for preparing osteotomies for the specific related implants.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1331-2020·2020-02-26
Siemens Luminos dRF Max Recalled for Collision Control Override Risk
Siemens is recalling 46 Luminos dRF Max devices because an override function can disable collision controls, creating a risk of collision with obstacles or persons.
Product
Luminos dRF Max, Model No. 10762471 - Product Usage: Luminos dRF Max is a device intended to visualize anatomical structures by converting an X-ray pattern into a visible image. The system has medical applications ranging from gastrointestinal examinations to cranial, skeletal…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1310-2020·2020-02-26
Nobel Biocare Tapered Drills Recalled Due to Sterility Concerns
Nobel Biocare is recalling 154 units of Tapered RP 4.3x13 mm drills because a packaging defect may compromise sterility.
Product
Drill Tapered RP 4.3x13 mm Single-Pat - Product Usage: The Guided Drills (Twist (Step) Drills, Guided Tapered Drills) are used for preparing osteotomies for the specific related implants.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1298-2020·2020-02-26
Polysorb Braided Absorbable Suture Recalled for Packaging Integrity Issues
Covidien LLC is recalling specific lots of Polysorb Braided Absorbable Suture due to potential packaging integrity issues that may impact the humidity or sterility barrier.
Product
Polysorb Braided Absorbable Suture 0 30" VIOLET GU-46, Item Code UL877 - Product Usage: Indicated for use in soft tissue approximation or ligation and ophthalmic surgery, but not in cardiovascular or neural tissue.
Category
Medical Device
Distribution
Distributed nationwide